Design, synthesis, molecular docking and cytotoxic activity of novel urea derivatives of 2-amino-3-carbomethoxythiophene
Author:
Funder
Foundation for the National Institutes of Health
Publisher
Springer Science and Business Media LLC
Subject
General Chemistry
Link
https://link.springer.com/content/pdf/10.1007/s12039-020-01834-w.pdf
Reference37 articles.
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5. Karp J E, Giles F J, Gojo I, Morris L, Greer J, Johnson B, Thein M, Sznol M and Low J 2008 A phase I study of the novel ribonucleotide reductase inhibitor 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP, Triapine®) in combination with the nucleoside analog fludarabine for patients with refractory acute leukemias and aggressive myeloproliferative disorders Leuk Res. 32 71
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